Association between Inflammatory Factors, Vitamin D, Long Non-Coding RNAs, MALAT1, and Adiponectin Antisense in Individuals with Metabolic Syndrome

Mol Nutr Food Res. 2023 Mar;67(5):e2200144. doi: 10.1002/mnfr.202200144. Epub 2023 Jan 26.

Abstract

Background: Metabolic syndrome (MetS) is a common clustering of cardiovascular risk factors associated with increased inflammation. Long non-coding RNA (LncRNA) are involved in many of the body's metabolic activities, including inflammation. Vitamin D may play a vital role in preventing metabolic syndrome risk factors. This study aimed to evaluate the status of inflammation and expression of LncRNA and their relationship with serum vitamin D levels in patients with metabolic syndrome.

Method: This cross-sectional study included staff and Mashhad University of Medical Sciences students between 30 and 50 years old who met the International Diabetes Federation criteria for Mets. Total RNA was extracted from both frozen clinical samples using the Trizol reagent.

Results: A total of eighty people were recruited into the two groups, with and without MetS. Inflammatory markers were higher in the individuals in the MetS group, and linear regression showed an inverse association between serum vitamin D and LncRNAs. There was a positive association between inflammatory biomarkers, lipid profiles and Adiponectin Antisense (APQ AS) expression.

Conclusion: APQ AS and MALAT1 levels are positively associated with inflammatory biomarkers and inverse relation between MALAT1 and serum 25 (OH) D concentration.

Keywords: MALAT1; inflammation; long noncoding RNA; metabolic syndrome; vitamin D.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biomarkers / blood
  • Female
  • Humans
  • Inflammation Mediators / blood
  • Male
  • Metabolic Syndrome* / diagnosis
  • Middle Aged
  • RNA, Long Noncoding / blood
  • Vitamin D / blood

Substances

  • Vitamin D
  • Biomarkers
  • RNA, Long Noncoding
  • ADIPOQ protein, human
  • MALAT1 long non-coding RNA, human
  • Inflammation Mediators